US3378408A - Electrolytic cell employing aluminum as negative electrode and an alkaline electrolyte containing hypochlorite anions - Google Patents

Electrolytic cell employing aluminum as negative electrode and an alkaline electrolyte containing hypochlorite anions Download PDF

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Publication number
US3378408A
US3378408A US437724A US43772465A US3378408A US 3378408 A US3378408 A US 3378408A US 437724 A US437724 A US 437724A US 43772465 A US43772465 A US 43772465A US 3378408 A US3378408 A US 3378408A
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cell
aluminum
electrolyte
plate
electrolytic cell
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US437724A
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Robert P Hamlen
Randall N King
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General Electric Co
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General Electric Co
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Priority to US437724A priority Critical patent/US3378408A/en
Priority to GB7353/66A priority patent/GB1095074A/en
Priority to JP1425066A priority patent/JPS4429940B1/ja
Priority to NL6602960A priority patent/NL6602960A/xx
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00—Primary cells; Manufacture thereof
    • H01M6/04—Cells with aqueous electrolyte

Definitions

  • Our invention relates to a new electrolytic cell and battery employing aluminum as a negative electrode and an alkaline electrolyte containing hypochlorite anions.
  • FIGURE 1 is a perspective view, partly in section, of a flat plate, back-to-back battery
  • FIGURE 2 is a vertical section of a spiral plate cell
  • FIGURE 3 is a plot of potential versus current density at various electrolyte values.
  • FIGURE 4 is a plot of potential versus current density at diifering temperatures.
  • the negative plate or electrode of a cell formed according to our invention is formed of aluminum. Any aluminum of commercial purity may be employed. Additionally the plate may be formed of any aluminum alloy generally known in the art to be the functional equivalent of aluminum in electrolytic cell performance. Alloys of aluminum and mercury, aluminum and zinc, and aluminum and magnesium, for example, are so disclosed in Use of Aluminum Anodes in Primary Batteries, S. Zaromb, Journal of the Electrochemical Society, 'vol. 109, No. 12. The metal may be employed in any convenient fabricating 3,378,408- Patented Apr. 16, 1968 form, such as a screen, foil, plate, etc. Since the aluminum is consumed during operation of the cell, the quantity of the aluminum present in the plates may be matched to the intended use of the cell.
  • the positive plate or electrode of the cell may be formed of any material lying lower in the electromotive series than aluminum and which will not be corroded during cell use.
  • Exemplary preferred materials include copper, stainless steel, carbon, nickel, oxide coated iron, etc. Since the positive plates are not consumed during cell operation, only minimal amounts of materials need be employed in cell fabrication.
  • the materials may be employed as separate elements in the form of a screen, foil, thin plate, etc., as in the case of the aluminum negative plate. It is preferred that the positive plate take the form of a thin layer attached to one side of the aluminum plate so that a bare minimum amount of positive plate metal may be employed. Thin films of metal may be laid down by various well-known techniques, such as chemical deposition, electroplating, pressure laminating, etc.
  • hypochlorite anions An aqueous electrolyte is employed containing hypochlorite anions.
  • Hypochlorite anions may be obtained by dissolving hypochlorous acid or any conveniently available salt thereof, such as laundry bleach (aqueous sodium hypochlorite commonly sold under the trademark Chlorox), bleaching powder or chlorinated lime (calcium chloride hypochlorite), etc. in water. It is preferred that the electrolyte be saturated with hypochlorite anions, although concentrations as low as 0.1 of saturation or lower may find utility.
  • the electrolyte be maintained alkaline.
  • hypochlorous acid or other acid or neutral source of hypochlorite anions it is necessary that an alkalizing agent be also present in the electrolyte to maintain the solution alkaline, preferably with a pH above 10.5.
  • alkalizing agents include alkali metal bicarbonates, carbonates, and hydroxides.
  • the electrolyte when the electrolyte is saturated with hypochlorite anions derived from alkali and alkaline earth hypochlorite salts or chlorinated lime, a pH in excess of 10.5 is imparted without resort to supplementary alkalizing agents.
  • a supplementary alkalizing agent in combination with an alkaline source of hypochlorite anions in order to increase the pH to an even higher alkaline value and to retain the pH after the hypochlorite concentration is reduced in use.
  • increase of the pH prevents aluminum oxide accumulation on the negative plates, at a higher pH the alkalizing agent may compete with the hypochlorite anion in attacking the aluminum.
  • the choice of proper electrolyte pH will depend to some extent on whether maximum cell capacity for a short period or low cell capacity for an extended period is desired. For most purposes an initial electrolyte pH ranging from 10.5 to 14 is preferred.
  • any number of well-known conventional configurations may be employed.
  • the positive electrode is not depleted during cell use.
  • cells featuring back-to-back plate constructions in which the positive plate is only a thin film on the negative plate are generally prefered.
  • any cell or battery construction include a port in the casing for adding electrolyte after cell assembly. Additionally, inasmuch as cells constructed according to our invention exhibit improved erformance at elevated temperatures up to approximately 100 C., it may be desired to incorporate into the cell or battery some means for increasing the temperature of the electrolyte.
  • FIGURE 1 An exemplary battery construction is depicted in FIGURE 1.
  • the battery includes an insulating casing 1 housing a plurality of back-to-back plates 2.
  • the plates are characterized as back-to-back since they are formed of an aluminum sheet 3 shown in cross section having adhered thereto a thin layer 4 of a noncorrosive metal having a lower position in the electromotive series than aluminum. Since the layers 4 are too thin to be shown in cross section, they are illustrated by heavy lines.
  • the end-most plates are each connected to terminals 5 which serve as the positive and negative battery terminals.
  • a port 6 is provided in the casing between each pair of plates.
  • a closure or plug 7 is mounted within each port.
  • the battery contains no electrolyte; however, electrolyte may be added through the ports when it is desired to place the battery in operation. It is appreciated that the closures or plugs will be loosely fitted or removed during cell portions so that any gaseous materials formed within the battery may be vented to the atmosphere.
  • FIG- URE 2 A spiral plate cell construction is illustrated in FIG- URE 2.
  • the cell includes an electrically conductive casing forming one terminal of the cell.
  • a winding spindle 21 formed of insulating material and having spirally wound thereon a four-layer assembly consisting of a first layer 22, which is an aluminum plate, a second layer 23 formed of a porous insulating spacer, a third layer 24 which is a plate formed of a metal occupying a lower position in the electromotive series than aluminum, and a fourth layer 25 which is a porous, insulating spacer.
  • the aluminum plate is connected to the cell casing through lead 28.
  • an insulating element 29 is mounted in the upper end of the conductive casing by crimping.
  • the element mounts a positive terminal 30 which is connected to the non-aluminum metal plate by lead 31.
  • a port 32 is provided in the insulating element for the admission of electrolyte to the cell. As shown, the port is provided with a plug 33.
  • the electrolyte is drawn between the plates by the capillary action of the porous, insulating spacers. Excess electrolyte fills the bottom of the casing and may extend upwardly into the winding spindle to a level 34 as illustrated.
  • FIGURES 1 and 2 The operation of the battery and cell illustrated in FIGURES 1 and 2, respectively, is essentially similar. The units are fully assembled except for the electrolyte and stored awaiting use. When the cell is required, it is placed into service by removal of the plug and the addition of electrolyte.
  • the FIGURE 1 battery is capable of yielding high voltage and high current for a short period or a high voltage and low current for a relatively longer period.
  • the cell shown in FIGURE 2 is capable of yielding a low voltage and high current for a short period or a low voltage and low current for a relatively longer period. Batteries such as shown in FIG- URE 1 may find utility as auxiliary car-starting batteries,
  • cells of the FIGURE 2 type may be used to operate emergency lighting.
  • a multiplicity of uses for cells and batteries constructed according to our invention will, of course, be apparent to one skilled in the art. Assuming that the aluminum plates are not depleted during any given use of a unit, the electrolyte may be removed and the unit again stored against future needs.
  • Examples 1-5 For each of five tests, a cell was constructed having one aluminum plate and one copper plate spaced therefrom A; inch. Each plate had a surface area of 1 in. in contact with the electrolyte. Tests were run at 25 C. The composition of the electrolyte for each test was formed as indicated in Table 1. Performance of each cell at a variety of current loads is indicated in FIGURE .3.
  • Electrolyte Components (g.) Test No NuaCOs CaCl(OCl) H10
  • Example 6 A cell was constructed as described in Examples 1-5. An electrolyte was employed formed by mixing 1 g. of lye with 32 g. of an aqueous solution consisting essentially of water and 5.25 percent by weight of sodium hypochlorite, based on the weight of the aqueous solution. The cell was operated at 25 C. The test results are plotted as Test No. 7 in FIGURE 3. The electrolyte pH was 13.0.
  • Example 8 The procedure of Example 7 was repeated, except that the lye content of the electrolyte was omitted. The test results are plotted as Test No. 8 in FIGURE 3. The electrolyte pH was 11.2.
  • Example 9- A cell was constructed as described in Examples 2-6. An electrolyte was used corresponding to the electrolyte employed in Test No. 1. The cell was operated at C. The test results are indicated as Test No. 6 in FIGURE 4. For purposes of comparison, Test No. 1 is also plotted in FIGURE 4.
  • Example 10 A strip of common aluminum window screen 1 and A inch wide by 12 inches long was laid out. A plastic screen of like dimension was placed on top of the aluminum screen and a copper window screen of like dimension was superimposed on the plastic screen. A second plastic screen identical to the first was placed on the copper screen. Each screen had approximately 14 strands per linear inch. The four screens were rolled into a spiral and electrical leads were attached to the copper and aluminum screens. The spiral placed in a ml. beaker and covered with an electrolyte formed of 8 g. of calcium chloride hypochlorite, 8 g. of sodium carbonate, and 64 g. of water. A current of 300 ma. was drawn from the cell at a potential of 1.2 volts for a period of one-half hour at 25 C. At the end of this period, the spiral was removed from the electrolyte and disassembled. The aluminum screen remained intact indicating a useful cell life well in excess of the test period.
  • An electrolytic cell comprising a casing
  • a negative electrode consisting essentially of aluminum
  • a positive electrode consisting essentially of a metal lower in the electromotive series than aluminum
  • an alkaline aqueous electrolyte consisting essentially of water, a source ofhypochlorite anions, and sufiicient alkalizing agent to maintain a pH in excess of 10.5, said electrolyte being saturated with hypochlorite anions.
  • said positive electrode consisting of copper.
  • An electrolytic battery including a casing
  • an alkaline aqueous electrolyte consisting essentially of water, a source of hypochlorite anions, and sufiicient alkalizing agent to maintain a pH in excess of 10.5, said electrolyte being saturated with hypochlorite anions, and said electrolyte lying between adjacent plates.
  • An electrolytic cell including acasing, a negative plate consisting essentially of aluminum, a positive plate consisting essentially of a metal lying lower in the electromotive series than aluminum, said plates being spirally wound and mounted within said casing, porous means insulating said plates, and an alkaline, aqueous electrolyte permeating said porous insulating means consisting essentially of water, a source of hypochlorite anions, and sufficient alkalizing agent to maintain a pH in excess of 10.5, said electrolyte being saturated with hypochlorite anions.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Primary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)
US437724A 1965-03-08 1965-03-08 Electrolytic cell employing aluminum as negative electrode and an alkaline electrolyte containing hypochlorite anions Expired - Lifetime US3378408A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US437724A US3378408A (en) 1965-03-08 1965-03-08 Electrolytic cell employing aluminum as negative electrode and an alkaline electrolyte containing hypochlorite anions
GB7353/66A GB1095074A (en) 1965-03-08 1966-02-18 Improvements in primary cells
JP1425066A JPS4429940B1 (enrdf_load_stackoverflow) 1965-03-08 1966-03-07
NL6602960A NL6602960A (enrdf_load_stackoverflow) 1965-03-08 1966-03-07

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US437724A US3378408A (en) 1965-03-08 1965-03-08 Electrolytic cell employing aluminum as negative electrode and an alkaline electrolyte containing hypochlorite anions

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JP (1) JPS4429940B1 (enrdf_load_stackoverflow)
GB (1) GB1095074A (enrdf_load_stackoverflow)
NL (1) NL6602960A (enrdf_load_stackoverflow)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3434886A (en) * 1965-06-29 1969-03-25 Philips Corp Primary cell
US3953239A (en) * 1975-01-27 1976-04-27 The United States Of America As Represented By The Secretary Of The Navy Al-AgO primary battery
US4320182A (en) * 1979-11-21 1982-03-16 General Electric Company Electrochemical cell having cast-in-place insulator
US4654963A (en) * 1979-11-21 1987-04-07 General Electric Company Method for making electrochemical cell having cast-in-place insulator
US20030161959A1 (en) * 2001-11-02 2003-08-28 Kodas Toivo T. Precursor compositions for the deposition of passive electronic features
US11139483B2 (en) 2019-10-03 2021-10-05 Andrei A. Gakh Pulsed aluminum battery
US20230076928A1 (en) * 2017-03-13 2023-03-09 Ifbattery Inc. Electrochemical Cells
US11952672B2 (en) 2018-09-12 2024-04-09 Ifbattery Inc. Series of cells for use in an electrochemical device

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US474454A (en) * 1892-05-10 Carl lxtcke
US1332485A (en) * 1919-03-26 1920-03-02 Universal Artificial Limb & Su Artificial hand and arm
US1412513A (en) * 1917-02-19 1922-04-11 Westinghouse Electric & Mfg Co Electrolyte
US1864652A (en) * 1925-05-15 1932-06-28 Nat Carbon Co Inc Primary cell and electrolyte therefor
US2180955A (en) * 1938-11-12 1939-11-21 Union Carbide & Carbon Corp Primary battery
US2229036A (en) * 1937-07-20 1941-01-21 Harry A Furman Electrode for sea water detection
US2543106A (en) * 1946-12-26 1951-02-27 Burgess Battery Co Deferred action primary battery
US2554447A (en) * 1949-01-26 1951-05-22 Gen Aniline & Film Corp Voltaic cell
US2667527A (en) * 1949-08-15 1954-01-26 Willard Storage Battery Co Deferred action battery
US2936327A (en) * 1954-02-18 1960-05-10 John P Schrodt Deferred activation battery

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US474454A (en) * 1892-05-10 Carl lxtcke
US1412513A (en) * 1917-02-19 1922-04-11 Westinghouse Electric & Mfg Co Electrolyte
US1332485A (en) * 1919-03-26 1920-03-02 Universal Artificial Limb & Su Artificial hand and arm
US1864652A (en) * 1925-05-15 1932-06-28 Nat Carbon Co Inc Primary cell and electrolyte therefor
US2229036A (en) * 1937-07-20 1941-01-21 Harry A Furman Electrode for sea water detection
US2180955A (en) * 1938-11-12 1939-11-21 Union Carbide & Carbon Corp Primary battery
US2543106A (en) * 1946-12-26 1951-02-27 Burgess Battery Co Deferred action primary battery
US2554447A (en) * 1949-01-26 1951-05-22 Gen Aniline & Film Corp Voltaic cell
US2667527A (en) * 1949-08-15 1954-01-26 Willard Storage Battery Co Deferred action battery
US2936327A (en) * 1954-02-18 1960-05-10 John P Schrodt Deferred activation battery

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3434886A (en) * 1965-06-29 1969-03-25 Philips Corp Primary cell
US3953239A (en) * 1975-01-27 1976-04-27 The United States Of America As Represented By The Secretary Of The Navy Al-AgO primary battery
US4320182A (en) * 1979-11-21 1982-03-16 General Electric Company Electrochemical cell having cast-in-place insulator
US4654963A (en) * 1979-11-21 1987-04-07 General Electric Company Method for making electrochemical cell having cast-in-place insulator
US20030161959A1 (en) * 2001-11-02 2003-08-28 Kodas Toivo T. Precursor compositions for the deposition of passive electronic features
US20230076928A1 (en) * 2017-03-13 2023-03-09 Ifbattery Inc. Electrochemical Cells
US11894591B2 (en) * 2017-03-13 2024-02-06 Ifbattery Inc. Electrochemical cells
US11952672B2 (en) 2018-09-12 2024-04-09 Ifbattery Inc. Series of cells for use in an electrochemical device
US11139483B2 (en) 2019-10-03 2021-10-05 Andrei A. Gakh Pulsed aluminum battery

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JPS4429940B1 (enrdf_load_stackoverflow) 1969-12-04
NL6602960A (enrdf_load_stackoverflow) 1966-09-09
GB1095074A (en) 1967-12-13

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